CAS 132292-17-2
:2-Naphthalenecarboxylic acid, 6-(4-methoxyphenyl)-
Description:
2-Naphthalenecarboxylic acid, 6-(4-methoxyphenyl)-, also known by its CAS number 132292-17-2, is an organic compound characterized by its naphthalene backbone substituted with a carboxylic acid group and a methoxyphenyl group. This compound typically exhibits properties associated with aromatic carboxylic acids, including moderate solubility in organic solvents and limited solubility in water due to its hydrophobic naphthalene structure. The presence of the methoxy group enhances its electron-donating characteristics, potentially influencing its reactivity and interactions in various chemical environments. It may participate in hydrogen bonding due to the carboxylic acid functional group, which can affect its physical properties such as melting and boiling points. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical and materials science research. Its structural features suggest potential applications in organic synthesis and as a building block for more complex molecules.
Formula:C18H14O3
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
6-(4-Methoxyphenyl)-2-naphthoic acid
CAS:Formula:C18H14O3Purity:97%Color and Shape:SolidMolecular weight:278.30206-(4-Methoxyphenyl)-2-naphthoic Acid
CAS:Controlled Product<p>Applications 6-(4-Methoxyphenyl)-2-naphthoic Acid is a reactant in the synthesis of Adapalene (A225000), a retinoid selective for retinoic acid receptor (RAR) subtypes β and γ. Antiacne.<br>References Milanese, A., et. al.: Bioorg. Chem., 39, 151 (2011); Griffiths, C.E.M., et al.: J. Invest. Dermatol., 101, 325 (1993); Bernard, B.A., et al.: Skin Pharmacol., 6, 61 (1993); Waugh, J., et al.: Drugs, 64, 1465 (2004)<br></p>Formula:C18H14O3Color and Shape:NeatMolecular weight:278.3
